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MIR4762 (microRNA 4762)

Identity

Alias_symbol (synonym)hsa-mir-4762
Other alias-
HGNC (Hugo) MIR4762
LocusID (NCBI) 100616253
Atlas_Id 69675
Location 22q13.31  [Link to chromosome band 22q13]
Location_base_pair Starts at 45760524 and ends at 45760598 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)MIR4762   41603
Cards
Entrez_Gene (NCBI)MIR4762  100616253  microRNA 4762
Aliases
GeneCards (Weizmann)MIR4762
Ensembl hg19 (Hinxton)ENSG00000264160 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264160 [Gene_View]  ENSG00000264160 [Sequence]  chr22:45760524-45760598 [Contig_View]  MIR4762 [Vega]
ICGC DataPortalENSG00000264160
TCGA cBioPortalMIR4762
AceView (NCBI)MIR4762
Genatlas (Paris)MIR4762
WikiGenes100616253
SOURCE (Princeton)MIR4762
Genetics Home Reference (NIH)MIR4762
miRBaseMIR4762
dbDEMCMIR4762
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4762  -     chr22:45760524-45760598 +  22q13.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4762  -     22q13.31   [Description]    (hg19-Feb_2009)
GoldenPathMIR4762 - 22q13.31 [CytoView hg19]  MIR4762 - 22q13.31 [CytoView hg38]
ImmunoBaseENSG00000264160
Mapping of homologs : NCBIMIR4762 [Mapview hg19]  MIR4762 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4762
Alternative Splicing GalleryENSG00000264160
Gene ExpressionMIR4762 [ NCBI-GEO ]   MIR4762 [ EBI - ARRAY_EXPRESS ]   MIR4762 [ SEEK ]   MIR4762 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4762 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616253
GTEX Portal (Tissue expression)MIR4762
Human Protein AtlasENSG00000264160-MIR4762 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4762
DMDM Disease mutations100616253
Blocks (Seattle)MIR4762
Human Protein Atlas [tissue]ENSG00000264160-MIR4762 [tissue]
Protein Interaction databases
FunCoupENSG00000264160
BioGRIDMIR4762
STRING (EMBL)MIR4762
ZODIACMIR4762
Ontologies - Pathways
Huge Navigator MIR4762 [HugePedia]
snp3D : Map Gene to Disease100616253
BioCentury BCIQMIR4762
ClinGenMIR4762
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616253
Clinical trialMIR4762
Miscellaneous
canSAR (ICR)MIR4762 (select the gene name)
DataMed IndexMIR4762
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4762
EVEXMIR4762
GoPubMedMIR4762
iHOPMIR4762
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Sep 3 15:54:23 CEST 2019

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